Abstract
The continuous combustion of conventional fossil fuels leads to undesirable environmental consequences. Increasing CO2 emissions and depletion of fossil fuels are two major concerns in today’s society. To combat these problems, we need to find an alternative source of energy that meet the current demands and at the same time has minimal effect on the environment. Electrochemical reduction of CO2 (ERCO2) provides a two-way solution as it results in a net decrease in the amount of CO2 in the atmosphere by capturing CO2 from the surroundings and converting it into fuels that can be used to source energy. This review presents the recent trends in the electrochemical reduction of CO2 to generate green fuel with an emphasis on reactor configurations, electrocatalysts, and solid polymer electrolytes. The influence of various functionalized catalysts and surface structures on ERCO2 is reviewed. Finally, the future perspectives on the progress of electrochemical reduction of CO2 will be presented.
Graphical Abstract
Abbreviations
- AEM:
-
Anion exchange membrane
- CD:
-
Current density
- CEM:
-
Cation exchange membrane
- CNT:
-
Carbon nanotube
- ERCO2 :
-
Electrochemical reduction of CO2
- FE:
-
Faradic efficiency
- GDL:
-
Gas diffusion layer
- HER:
-
Hydrogen evolution reaction
- MOF:
-
Metal–organic frameworks
- MOP:
-
Metal–organic porous
- NP:
-
Nanoparticles
- PEI:
-
Polyethyleneimine
- PVA:
-
Polyvinyl alcohol
- SPE:
-
Solid polymer electrolyte
- SPEEK:
-
Sulphonated poly(etheretherketone)
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Acknowledgements
The authors gratefully acknowledge the financial support of the Science and Engineering Research Board (SERB), Department of Science and Technology (DST), Government of India, under its Early Career Research Award Scheme vide sanction order No. ECR/2016/001340, dated 15.03.2017 and ECR/2016/001844, dated – 23/03/2017.
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Kumar, A., Aeshala, L.M. & Palai, T. Electrochemical reduction of CO2 to useful fuel: recent advances and prospects. J Appl Electrochem 53, 1295–1319 (2023). https://doi.org/10.1007/s10800-023-01850-x
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DOI: https://doi.org/10.1007/s10800-023-01850-x